A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118223



Internal ID21301489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24704591..24774513hg38UCSC Ensembl
Innerchr3:24746082..24816004hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3869923
hg1969923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105568, nssv14104555, nssv14107833, nssv14108306
Samplessample285, sample91, sample416, sample233
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118223
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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